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Walgreens Urinary Pain Relief Maximum Strength (Walgreens Co.)

Available Formats

Dosage Form Package Information Links
TABLET 1 BLISTER PACK in 1 CARTON (0363-0113-01) > 12 TABLET in 1 BLISTER PACK (0363-0113-12) Label Information

Complete Walgreens Urinary Pain Relief Maximum Strength Information

  • ACTIVE INGREDIENT

    PHENAZOPYRIDINE HYDROCHLORIDE   97.5 MG


  • PURPOSE

    PHENAZOPYRIDINE HYDROCHLORIDE                     URINARY ANALGESIC


  • WARNINGS

    DO NOT EXCEED RECOMMENDED DOSAGE


  • ASK DOCTOR

    ASK DOCTOR BEFORE USE

    IF YOU HAVE KIDNEY DISEASE

    ALLERGIES TO FOODS,PRESERVATIVES OR DYES

    HAD A HYPERSENSITIVE REACTION TO PHENAZOPYRIDINE


  • WHEN USING

    WHEN USING THIS PRODUCT

    STOMACH UPSET MAY OCCUR,TAKING THIS PRODUCT WITH OR AFTER MEALS MAY REDUCE STOMACH UPSET

    YOUR URINE WILL BECOME REDDISH ORANGE IN COLOR.THIS IS NOT HARMFUL,BUT CARE SHOULD BE TAKEN TO

    AVOID STAINING CLOTHING OR OTHER ITEMS.


  • STOP USE

    STOP USE AND ASK A DOCTOR

    IF YOUR SYMPTOMS LAST FOR MORE THAN 2 DAYS

    YOU SUSPECT YOU ARE HAVING AN ADVERSE REACTION TO THE MEDICATION


  • PREGNANCY OR BREAST FEEDING

    ASK A HEALTH PROFESSIONAL BEFORE USE


  • KEEP OUT OF REACH OF CHILDREN

    IN CASE OF OVERDOSE ,GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.


  • INDICATIONS & USAGE

    Use; fast relief from urinary pain,burning,urgency and frequency associated with urinary tract infections.


  • INACTIVE INGREDIENT

    Lactose, magnesium silicate, magnesium stearate, microcrystalline cellulose,

    pharmaceutical glaze, and sodium starch glycolate.


  • DOSAGE & ADMINISTRATION

    Adults and Children 12 years of age and over; take 2 tablets 3 times daily with a full glass of water,with or after meals as needed.

    Children under 12 years of age; consult a doctor.

    Do not use for more than 2 days ( 12 tablets ) without consulting a Doctor.


  • INGREDIENTS AND APPEARANCE
    WALGREENS URINARY PAIN RELIEF MAXIMUM STRENGTH 
    phenazopyridine hydrochloride tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0113
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHENAZOPYRIDINE HYDROCHLORIDE (UNII: 0EWG668W17) (PHENAZOPYRIDINE - UNII:K2J09EMJ52) PHENAZOPYRIDINE HYDROCHLORIDE 97.5 mg
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM SILICATE (UNII: 9B9691B2N9)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Color red Score no score
    Shape ROUND Size 7mm
    Flavor Imprint Code 975
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0363-0113-01 1 in 1 CARTON
    1 NDC:0363-0113-12 12 in 1 BLISTER PACK
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 04/05/2010
    Labeler - Walgreens Co. (008965063)
    Registrant - Reese Pharmaceutical Co (004172052)
    Establishment
    Name Address ID/FEI Business Operations
    Reese Pharmaceutical Co 004172052 relabel, repack